A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005822



Internal ID19095039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:22867399..23011996hg38UCSC Ensembl
Innerchr4:22869022..23013619hg19UCSC Ensembl
Innerchr4:22478120..22622717hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38144598
hg19144598
hg18144598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620582
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005822
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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